Sirenidae
Temporal range:
Late Cretaceous - Present,
Siren intermedia
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Urodela
Family: Sirenidae
Gray, 1825
Genera

  Habrosaurus
  Pseudobranchus
  Siren

Sirenidae, the sirens, are a family of neotenic aquatic salamanders. Family members have very small fore limbs and lack hind limbs altogether.[1] In one species, the skeleton in their fore limbs is made of only cartilage. In contrast to most other salamanders, they have external gills bunched together on the neck in both larval and adult states. Sirens are found only in the Southeastern United States and northern Mexico.[1]

Although they are primarily carnivorous, they are the only salamanders observed eating plant material.[2]

Description

Sirens are quite distinct from other salamanders, and in some classifications they form their own suborder, Sirenoidea, or as a completely distinct order (Meantes or Trachystomata). Genetic analysis variously places them as the sister to other Salamandroidea[3][4] or as sister to all other salamanders.[5] Many of their unique characteristics seem to be partly primitive and partly derivative.

Sirens are generally eel-like in form, with two tiny, but otherwise fully developed, fore limbs. They range from 25–95 cm (9.8–37.4 in) in length.[1] They are neotenic, although the larval gills are small and functionless at first, and only adults have fully developed gills. Because of this, sirens most likely have evolved from a terrestrial ancestor that still had an aquatic larval stage. Like amphiumas, they are able to cross land on rainy nights.

Except for some patches of small teeth on their palates and on the splenial bone on the inner side of their lower jaws, their mouths have lost all dentition and have been replaced with a horny sheath that resembles a beak. Sirens are omnivorous, feeding mainly on worms, small snails, shrimps, and filamentous algae.[6] They are notable among salamanders (and most amphibians, aside from a few frog species) due to their semi-herbivorous habits.[2]

If the conditions of a water source are unsuitable, a larva will shrink its gills to mere stumps, and these may not function at all.[6] They are also able to burrow into mud of drying ponds and encase themselves with a cocoon of mucus to survive periods of drought.[1] During such periods, they breathe with their small but functional lungs.

Unlike other salamanders, an interventricular septum is present in the heart. At least two of the species can produce vocalizations.

The structure of sirens' reproductive systems suggests they employ external fertilization.[1] This has finally been confirmed in captive breeding experiments, showcasing that males also engage in parental care, building nests for their offspring.[7] Parental care among sirens is paternal due to external fertilization. In S. intermedia males circle around females and may rub or bite her flank region.[7] Both male and female will go on their backs and turn. It is assumed here where the female spawns and the male fertilizes her eggs.[7] After the courtship is over, the female leaves and the male guards the eggs. Males could potentially guard more than one brood, but they are known to bite females who enter a nesting site.[7] In other salamander families where external fertilization is used, paternal care has been observed.[7] This is critical to phylogeny, as most salamander families use external fertilization which may be pair with maternal care, meaning that sirens are one of the oldest groups of salamanders.[7]

The combined biomass of Siren intermedia species in a Texas pond exceeded the total biomass of the pond's seven species of fish.[8]

Taxonomy

The siren family (Sirenidae) is subdivided into five genera, three extinct, and two extant with two and three extant species, respectively:

References

  1. 1 2 3 4 5 Lanza, B., Vanni, S., & Nistri, A. (1998). Cogger, H.G. & Zweifel, R.G. (ed.). Encyclopedia of Reptiles and Amphibians. San Diego: Academic Press. pp. 69–70. ISBN 0-12-178560-2.{{cite book}}: CS1 maint: multiple names: authors list (link)
  2. 1 2 Hill, R. L., Mendelson, J. R. & Stabile, J. L. 2015. Direct observation and review of herbivory in Sirenidae (Amphibia: Caudata). Southeastern Naturalist 14, N5-N9.
  3. K. Roelants, D.J. Gower, M. Wilkinson, S.P. Loader, S.D. Biju, K. Guillaume, L. Moriau, F. Bossuyt (2007) Global pattern of diversification in the history of modern amphibians. Proc. Natl. Acad. Sci. USA, 104: 887-892
  4. R. Alexander Pyron; John J. Wiens (2011). "A large-scale phylogeny of Amphibia including over 2800 species, and a revised classification of extant frogs, salamanders, and caecilians". Molecular Phylogenetics and Evolution. 61 (2): 543–583. doi:10.1016/j.ympev.2011.06.012. PMID 21723399.
  5. Peng Zhang, David B.Wake (2009) Higher-level salamander relationships and divergence dates inferred from complete mitochondrial genomes. Molecular Phylogenetics and Evolution 53: 492-508
  6. 1 2 John Farrand Jr., The Audubon Society Encyclopedia of Animal Life, 1982
  7. 1 2 3 4 5 6 Reinhard, S., Voitel, S. & Kupfer, A. 2013. External fertilisation and paternal care in the paedomorphic salamander Siren intermedia Barnes, 1826 (Urodela: Sirenidae). Zoologischer Anzeiger 253, 1-5.
  8. Gehlbach, Frederick R.; Kennedy, Stephen E. (1978). "Population Ecology of a Highly Productive Aquatic Salamander (Siren intermedia)". The Southwestern Naturalist. 23 (3): 423–429. doi:10.2307/3670250. ISSN 0038-4909. JSTOR 3670250.
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